This approach demonstrates high efficiency in synthesizing acylmethylated pyrrolo[1,2-a]indoles, suggesting potential in organic synthesis.
A visible‐light‐promoted sequential radical acylmethylation/annulation of unactivated alkenes with sulfoxonium ylides has been developed, furnishing a range of acylmethylated pyrrolo[1,2‐ a ]indoles in high efficiency under photoredox conditions. Notably, this reaction is characterized by mild conditions, operational simplicity, a wide substrate scope, and excellent functional group tolerance.
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Wu et al. (2025) studied this question.
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